Drug Eluting Stents Beat Bare Metal Stents In Diabetics

Main Category: Diabetes
Also Included In: Cardiovascular / Cardiology;  Clinical Trials / Drug Trials
Article Date: 12 Nov 2008 - 0:00 PDT

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Drug-eluting stents reduced the risk of revascularization, heart attack and death in diabetics as compared with bare-metal stents in the largest observational comparison, researchers reported at the American Heart Association's Scientific Sessions 2008. The results from The Drug-eluting and Bare Metal Stenting in Patients with Diabetes Mellitus: Results from the Mass-DAC Registry, were presented as a late-breaking clinical trial. The study is simultaneously published in Circulation: Journal of the American Heart Association.

"We actually saw a significant benefit from using drug-eluting stents in this patient population," said Laura Mauri, M.D., M.Sc., principal investigator of the study and assistant professor of medicine at Brigham and Women's Hospital and Harvard Medical School in Boston, Mass. "First, they significantly reduced the need for repeat procedures which included repeat stenting or bypass surgery. Second, they were associated with lower rates of death and heart attack. So, as a result we can say that these stents appear to be safe in diabetic patients, whose diabetes puts them at higher risk of mortality and heart attack than the general population."

People with diabetes make up about a third of all patients undergoing percutaneous coronary interventions (PCI) to reopen blocked blood vessels. In PCI with stenting, a balloon-tipped catheter is threaded into the artery to the point of blockage. Then, the balloon is inflated to open the vessel and a mesh metal stent -- either bare-metal (BMS) or drug-eluting (DES) -- is inserted to keep the channel open. DES are coated with a drug that fights the proliferation of cells that can block the artery (called stenosis).

In the largest population-based comparison of stents in diabetics, researchers used data from a mandatory state registry. They identified 5,051 diabetics who underwent PCI at acute-care, non-federal hospitals between April 2003 and September 2004. Diabetic patients at those hospitals were about twice as likely to get DES compared to BMS (66.1 percent vs. 33.9 percent), researchers said.

At three years of follow-up, the unadjusted cumulative endpoint of death was 14.4 percent for DES patients compared to 22.2 percent for BMS patients, Mauri said.

The researchers then matched a subset of 1,476 DES and 1,476 BMS patients to control for 63 potential confounders such as concurrent conditions and medications. In that comparison, they found the risk-adjusted mortality at three years was 17.5 percent for DES patients vs. 20.7 percent, a small but significant 3.2 percent absolute reduction in mortality in DES patients, with no excess adverse events. The choice of BMS or DES was not randomized, but was done at the direction of the treating physician, so it is possible that the patients given DES were different in the number of blood vessel or other characteristics.

Although three-year data were not yet available for rates of heart attack and target vessel revascularization, at two years of follow-up those rates were lower in the DES group compared to the BMS group.

"Diabetic patients represent a large and growing proportion of patients who undergo stenting," Mauri said. "We know that patients with diabetes have a higher incidence of adverse events following the procedure, including higher rates of restenosis (reblockage), heart attack and death related to heart problems."

"Previous studies indicated that drug-eluting stents reduce the rate of restenosis, but there has been controversy about their safety because of conflicting evidence from smaller studies."

Some of those studies found higher mortality associated with DES while others found no safety differences between the two types of stents. This study showed lower mortality and adverse events.

The Massachusetts Data Analysis Center (Mass-DAC) registry is a special resource to research outcomes after PCI, since the state department of public health requires that every non-federal hospital provide procedural information and outcomes for every adult who undergoes PCI. Such data are intended to monitor and to improve the quality of patient care.

"Through an effort headed by the Division of Health Care Quality at the Massachusetts Department of Public Health, we were able to use clinical data collected from every non-federal hospital in the state that treats patients with stents to monitor safety of the drug-eluting stents," said Sharon-Lise Normand, Ph.D., co-author of the study, director of the Mass-DAC and professor of health care policy (biostatistics) at Harvard Medical School and Harvard School of Public Health. "Surveillance systems such as this are critical to assessing quality and safety in the real-world."

Other co-authors are: Pallav Garg, M.B.B.S., M.Sc.; Treacy S. Silbaugh, B.Sc.; Robert E. Wolf, M.S.; Katya Zelevinsky, B.A.; Ann F. Lovett, R.N., M.A.; Manu R. Varma, B.S.; and Zheng Zhou, M.D., Ph.D. Individual author disclosures are available on the abstract.

The study was funded by Massachusetts Department of Public Health Contract 620022A4PRE.

Statements and conclusions of study authors that are presented at American Heart Association scientific meetings are solely those of the study authors and do not necessarily reflect association policy or position. The association makes no representation or warranty as to their accuracy or reliability. The association receives funding primarily from individuals; foundations and corporations (including pharmaceutical, device manufacturers and other companies) also make donations and fund specific association programs and events. The association has strict policies to prevent these relationships from influencing the science content. Revenues from pharmaceutical and device corporations are available at http://www.americanheart.org/corporatefunding.

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